4.5 Article

In-depth analysis of the relationship between bovine intestinal organoids and enteroids based on morphology and transcriptome

Journal

Publisher

WILEY
DOI: 10.1002/term.3351

Keywords

crypt; enteroid; fetal bovine; intestine; organoid; transcriptome

Funding

  1. China Agriculture Research System of MOF and MARA [CARS-37]
  2. Natural Science Foundation of Henan Province, China [212300410355]

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Intestinal organoids and enteroids are excellent models for studying intestinal functions, drug screening, and regenerative medicine. However, there have been few comparative studies on these models, especially in immunity and metabolism. Our study compared the transcriptome of organoids and enteroids and verified some of the results. We found that organoids and enteroids carry out different functions in immunity and metabolism, with organoids being more comprehensive and enteroids being suitable for immune and cancer research.
Intestinal organoids and enteroids as excellent models are miniaturized and simplified for studying intestinal physiological and pathological functions, drug screening, and regenerative medicine. Recently, the application demands for organoids and enteroids in organ development and nutrition metabolism, immune and cancer research increased. But there are few comparative studies on both of them, especially in immunity and metabolism, which is also conducive to further clarifying the role of crypt stem cells and stromal cells. In our study, natural organoids were obtained by tissue culture from fetal bovine jejunum and enteroids were successfully isolated and cultured from organoids without supplementing exogenous factors and Matrigel. These mini-guts displayed similar features to the intestine through immunohistochemistry and transmission electron microscopy. Organoid and enteroid were systematically compared based on the transcriptome. And some of the results were verified by qRT-PCR. Our results showed KDGs (Key driver genes) (e.g., SLC13A1, HOXA7, HOXA6, HOXA5, and HOXD4) of organoids enriched in signaling pathways related to organ development and morphology and metabolism. KDGs (e.g., IL-6, PTGS2, CDH1, JUN, and EGFR) of enteroid were involved in cancer, MAPK, and immune-related signaling pathways. To the Wnt signaling pathway, highly expressed genes in organoids, including RSPO2, NOTUM, WNT6, and RSPO3, supported the homeostasis of crypt stem cells. Enteroids highly expressed CTNNB1 and WNTs. In addition, we found that organoids and enteroids carried out different functions in immunity and metabolism due to different cell compositions. Therefore, it suggested organoid is more compatible and comprehensive, and enteroid is qualified for the research of immunity and cancer.

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